CA1283898C - Methode de preparation d'hydrocarbures liquides - Google Patents

Methode de preparation d'hydrocarbures liquides

Info

Publication number: CA1283898C
Authority: CA; Canada
Prior art keywords: catalyst; process according; molar ratio; mordenite; preparation
Prior art date: 1985-12-23
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

CA000523706A

Other languages

English (en)

Inventor

Gilbert Germaine

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Shell Canada Ltd

Original Assignee

Shell Canada Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-12-23

Filing date

1986-11-25

Publication date

1991-05-07

1986-11-25 Application filed by Shell Canada Ltd filed Critical Shell Canada Ltd

1991-05-07 Application granted granted Critical

1991-05-07 Publication of CA1283898C publication Critical patent/CA1283898C/fr

2008-05-07 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 33
229930195733 hydrocarbon Natural products 0.000 title claims abstract description 19
150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 19
238000002360 preparation method Methods 0.000 title claims abstract description 14
239000007788 liquid Substances 0.000 title claims abstract description 13
239000003054 catalyst Substances 0.000 claims abstract description 41
229910052751 metal Inorganic materials 0.000 claims abstract description 27
239000002184 metal Substances 0.000 claims abstract description 27
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 22
229910052759 nickel Inorganic materials 0.000 claims abstract description 11
239000000203 mixture Substances 0.000 claims abstract description 9
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 8
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
239000004411 aluminium Substances 0.000 claims description 5
229910052782 aluminium Inorganic materials 0.000 claims description 5
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
229910052680 mordenite Inorganic materials 0.000 claims description 5
229910052710 silicon Inorganic materials 0.000 claims description 4
239000010703 silicon Substances 0.000 claims description 4
229910052742 iron Inorganic materials 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 2
229910052804 chromium Inorganic materials 0.000 claims description 2
239000011651 chromium Substances 0.000 claims description 2
229910052733 gallium Inorganic materials 0.000 claims description 2
238000005342 ion exchange Methods 0.000 claims description 2
229910052703 rhodium Inorganic materials 0.000 claims description 2
239000010948 rhodium Substances 0.000 claims description 2
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 2
229910052706 scandium Inorganic materials 0.000 claims description 2
SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract description 12
150000002739 metals Chemical class 0.000 abstract description 8
230000000737 periodic effect Effects 0.000 abstract description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 3
150000001336 alkenes Chemical class 0.000 description 5
-1 alkali metal- Chemical class 0.000 description 4
238000009835 boiling Methods 0.000 description 4
239000000243 solution Substances 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000007789 gas Substances 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
238000012360 testing method Methods 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000013078 crystal Substances 0.000 description 2
238000011068 loading method Methods 0.000 description 2
229910052914 metal silicate Inorganic materials 0.000 description 2
239000002245 particle Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical class CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical class CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical class CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 1
IRUDSQHLKGNCGF-UHFFFAOYSA-N 2-methylhex-1-ene Chemical class CCCCC(C)=C IRUDSQHLKGNCGF-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229940037003 alum Drugs 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
239000002199 base oil Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000004523 catalytic cracking Methods 0.000 description 1
238000004517 catalytic hydrocracking Methods 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000004927 clay Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229940000425 combination drug Drugs 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
238000006317 isomerization reaction Methods 0.000 description 1
238000002386 leaching Methods 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
150000005673 monoalkenes Chemical class 0.000 description 1
AIYYMMQIMJOTBM-UHFFFAOYSA-L nickel(ii) acetate Chemical compound [Ni+2].CC([O-])=O.CC([O-])=O AIYYMMQIMJOTBM-UHFFFAOYSA-L 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000006384 oligomerization reaction Methods 0.000 description 1
239000008188 pellet Substances 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical class CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052712 strontium Inorganic materials 0.000 description 1
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
238000004227 thermal cracking Methods 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Crystallography & Structural Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Catalysts (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Medicinal Preparation (AREA)

CA000523706A 1985-12-23 1986-11-25 Methode de preparation d'hydrocarbures liquides Expired - Fee Related CA1283898C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB858531628A GB8531628D0 (en)	1985-12-23	1985-12-23	Preparation of liquid hydrocarbon
GB8531628		1985-12-23

Publications (1)

Publication Number	Publication Date
CA1283898C true CA1283898C (fr)	1991-05-07

Family

ID=10590186

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000523706A Expired - Fee Related CA1283898C (fr)	1985-12-23	1986-11-25	Methode de preparation d'hydrocarbures liquides

Country Status (9)

Country	Link
EP (1)	EP0233382B1 (fr)
JP (1)	JPH07103381B2 (fr)
AT (1)	ATE71928T1 (fr)
AU (1)	AU586722B2 (fr)
CA (1)	CA1283898C (fr)
DE (1)	DE3683631D1 (fr)
GB (1)	GB8531628D0 (fr)
SG (1)	SG44493G (fr)
ZA (1)	ZA869451B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8704960D0 (en) *	1987-03-03	1987-04-08	Shell Int Research	Catalytic conversion of olefins-containing feed
GB8806675D0 (en) *	1988-03-21	1988-04-20	Shell Int Research	Process for preparing liquid hydrocarbons
GB8916103D0 (en) *	1989-07-13	1989-08-31	Shell Int Research	Preparation and use of metal-containing zeolitic catalysts

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1135938A (en) *	1965-12-22	1968-12-11	Union Carbide Corp	Hydrocarbon conversion
GB1216272A (en) *	1968-02-27	1970-12-16	British Petroleum Co	Dimerisation of olefins
US3542671A (en) *	1968-05-09	1970-11-24	Universal Oil Prod Co	Hydroisomerization of olefins to isoparaffins
US4209499A (en) *	1977-10-21	1980-06-24	Mobil Oil Corporation	Crystalline zeolite ZSM-43 synthesis thereof
JPS56160316A (en) *	1980-05-14	1981-12-10	Toa Nenryo Kogyo Kk	Synthetic crystalline aluminosilicate composition and its manufacture
US4423269A (en) *	1981-09-25	1983-12-27	Chevron Research Company	Oligomerization of gaseous olefins
JPS5888325A (ja) *	1981-11-20	1983-05-26	Idemitsu Kosan Co Ltd	炭化水素の転化法
NL8301747A (nl) *	1983-05-17	1984-12-17	Shell Int Research	Werkwijze voor de bereiding van middeldestillaten.
US4554396A (en) *	1984-09-18	1985-11-19	Mobil Oil Corporation	Olefin upgrading with ferrosilicate zeolite catalyst
US4705907A (en) *	1985-05-29	1987-11-10	Showa Shell Sekiyu Kabushiki Kaisha	Production of liquid hydrocarbon from gas containing lower hydrocarbon

1985
- 1985-12-23 GB GB858531628A patent/GB8531628D0/en active Pending
1986
- 1986-11-25 CA CA000523706A patent/CA1283898C/fr not_active Expired - Fee Related
- 1986-12-03 EP EP86202161A patent/EP0233382B1/fr not_active Expired - Lifetime
- 1986-12-03 AT AT86202161T patent/ATE71928T1/de not_active IP Right Cessation
- 1986-12-03 DE DE8686202161T patent/DE3683631D1/de not_active Expired - Lifetime
- 1986-12-17 AU AU66640/86A patent/AU586722B2/en not_active Ceased
- 1986-12-17 JP JP61299086A patent/JPH07103381B2/ja not_active Expired - Lifetime
- 1986-12-17 ZA ZA869451A patent/ZA869451B/xx unknown
1993
- 1993-04-14 SG SG44493A patent/SG44493G/en unknown

Also Published As

Publication number	Publication date
DE3683631D1 (de)	1992-03-05
AU6664086A (en)	1987-06-25
AU586722B2 (en)	1989-07-20
ATE71928T1 (de)	1992-02-15
SG44493G (en)	1993-06-25
JPH07103381B2 (ja)	1995-11-08
EP0233382B1 (fr)	1992-01-22
GB8531628D0 (en)	1986-02-05
JPS62148592A (ja)	1987-07-02
EP0233382A1 (fr)	1987-08-26
ZA869451B (en)	1987-07-29

Legal Events

Date	Code	Title	Description
2003-05-07	MKLA	Lapsed

Publication	Publication Date	Title
EP0259954B1 (fr)	1990-11-14	Procédé de conversion d'hydrocarbures aliphatiques en C2 à C12 en hydrocarbures aromatiques sur une zéolite activée par zinc
KR920002241B1 (ko)	1992-03-20	저급지방족 탄화수소의 제조방법
CA1315299C (fr)	1993-03-30	Procede pour la preparation d'hydrocarbures liquides
EP0212850A1 (fr)	1987-03-04	Procédé de déshydrogénation et catalyseur
EP0332243B1 (fr)	1993-05-19	Procédé pour préparer des hydrocarbures normalement liquides à partir d'une charge d'hydrocarbures contenant des oléfines linéaires et ramifiées
US5659099A (en)	1997-08-19	Activated zeolite beta and its use for hydrocarbon conversion
US4252636A (en)	1981-02-24	Catalyst and process for conversion of hydrocarbons
US3669903A (en)	1972-06-13	Catalytic cracking process
EP0184461B1 (fr)	1989-07-26	Post traitement d'une composition catalytique à base d'un tamis moléculaire cristallin AMS 1B
CA1283898C (fr)	1991-05-07	Methode de preparation d'hydrocarbures liquides
US3915893A (en)	1975-10-28	Amorphous hydrocarbon conversion catalysts and process for preparing same
US6124228A (en)	2000-09-26	Mazzite supported catalyst
US3867305A (en)	1975-02-18	Amorphous hydrocarbon conversion catalysts and process for preparing same
US3962367A (en)	1976-06-08	Olefin isomerization using a cobalt-sulfur catalyst
CA1297501C (fr)	1992-03-17	Procede de conversion catalytique en deux temps de matieres olefiniques
CA1091638A (fr)	1980-12-16	Catalyseur et procede de transformation des hydrocarbures
JPS6316367B2 (fr)	1988-04-08
CA1083609A (fr)	1980-08-12	Hydroalkylation du benzene et de ses analogues
AU701283B2 (en)	1999-01-21	Process for upgrading a paraffinic feedstock
KR102769760B1 (ko)	2025-02-20	올리고머화 촉매의 스테이지-맞춤화된 교환에 의한 올리고머화 방법
EP0408153B1 (fr)	1993-10-20	Préparation et application de catalyseurs zéolitiques contenant des métaux
KR102786145B1 (ko)	2025-03-26	반응기에 충전하기 전 촉매의 건식 처리에 의한 올리고머화 방법
US4777311A (en)	1988-10-11	Process for converting C5 olefins to aromatic hydrocarbons and lighter olefins
US3113979A (en)	1963-12-10	Process for the isomerization of alkyl benzenes
JPH0819426B2 (ja)	1996-02-28	低級炭化水素の重質化方法